Systems, methods, and apparatuses for analyzing galvanic skin response based on exposure to electromagnetic and mechanical waves

ABSTRACT

Systems, methods, apparatus, and non-transitory computer readable media for measuring and analyzing galvanic skin response. Responses to stimuli including electromagnetic waves and mechanical waves, as well as substances exposed to electromagnetic waves and mechanical waves, are recorded and analyzed. Electromagnetic waves and mechanical waves are constructed based on biological outputs in one embodiment.

CROSS REFERENCES TO RELATED APPLICATIONS

This application is related to and claims priority from the following USpatents and patent applications. This application claims the benefit ofU.S. Provisional Application No. 62/829,313, filed Apr. 4, 2019, whichis incorporated herein by reference in its entirety. This application isalso a continuation-in-part of U.S. application Ser. No. 16/678,121filed Nov. 8, 2019, which claims the benefit of U.S. Provisional PatentApplication No. 62/758,599, filed Nov. 11, 2018, each of which isincorporated herein by reference in its entirety.

BACKGROUND OF THE INVENTION 1. Field of the Invention

The present invention relates to devices, methods, and systems formeasuring galvanic skin response based on exposure to stimuli includingelectromagnetic waves and mechanical waves and substances exposed toelectromagnetic waves and mechanical waves.

2. Description of the Prior Art

It is generally known in the prior art to expose subjects to lightand/or sound as part of a therapeutic process. It is also generallyknown to alter the structure of substances using energy including lightand/or sound. Methods and systems for measuring galvanic skin responseare also known. One application of galvanic skin response is to measureelectrical properties of acupuncture points. Dr. Reinhard Voll, a Germanphysician and engineer, developed a method of measuring galvanic skinresponse known as Electroacupuncture According to Voll (EAV) in the1940s.

Representative prior art patent documents include the following:

U.S. Pat. No. 5,830,140 for apparatus and method for registeringsubstance-specific and organism-specific energetic information byinventors Dillinger, et al., filed Nov. 22, 1995 and issued Nov. 3,1998, is directed to substance-specific and body-specific information inthe form of electromagnetic noise stored after separation with bandpassfilters so that individual noise spectra segments can reflect thedifferent planes of the body system and stored information of this typecan be combined with a carrier and used for therapy or used directly toactivate an alcohol/water mixture and produce a homeopathic medicament.

U. S. Publication No. 20020059247 for method of and apparatus forregistering and reproducing homeopathic information by inventorsDillinger, et al., filed Jun. 28, 2001 and published May 16, 2002, isdirected to homeopathic information in the form of electromagneticspectra or combinations of spectra or spectra sums downloaded through aglobal communication network from a site to a terminal and are used toproduce homeopathic medicaments or test substances or for treatment ofthe patient. The homeopathic data is stored and reproduced by musicstorage and communication formats, especially MP3.

U.S. Pat. No. 9,330,680 for Biometric-music interaction methods andsystems by inventors Kassam, et al., filed Sep. 9, 2013 and issued May3, 2016, is directed to a system and method for the automatic,procedural generation of musical content in relation to biometric data.The systems and methods use a user's device, such as a cell phone tocapture image data of a body part, and derive a biometric signal fromthe image data. The biometric signal includes biometric parameters,which are used by a music generation engine to generate music. The musicgeneration can also be based on user-specific data and quality datarelated to the biometric detection process.

U.S. Publication No. 20170007847 for Bioresonance frequency emittingdevice, system, and method by inventors Gross, et al., filed Jul. 7,2016 and published Jan. 12, 2017, is directed to a phototherapy or BRTprocess and apparatus, which, using a pre-recorded bioresonancefrequency or compilation of frequencies, causes an EMR emitter to emitwithin a biological window of a target organism to positively ornegatively affect the organism. The EMR may be generated in one or moreLEDs by a device connected to a controller of the EMR emitter whichdevice provides the pre-recorded bioresonance frequency or compilationof frequencies to control the LEDs' emitted light in terms of itsintensity and/or a frequency or flicker-rate.

U.S. Pat. No. 9,888,884 for Method of sonifying signals obtained from aliving subject by inventors Chafe, et al., filed Dec. 1, 2014 and issuedFeb. 13, 2018, is directed to a digital processor system that obtains atleast one time-domain signal representing brain activity and at leastone time-domain signal representing heart activity, each having atime-varying signal value. The system produces representations of aplurality of acoustic signals, each of which corresponds to a respectivetime-domain signal and is produced by concurrently generating aplurality of acoustic parameters, including a plurality of time-varyingacoustic parameters. One or more of the plurality of time-varyingacoustic parameters is modulated in accordance with at least the signalvalue of the respective time-domain signal. Each representation of anacoustic signal of the plurality of acoustic signals is further producedby combining the concurrently generated plurality of acoustic parametersto produce the representation of the acoustic signal corresponding tothe respective time-domain signal. The system combines therepresentations of each of the plurality of acoustic signals to producea combined acoustic signal.

U. S. Publication No. 20040087838 for meridian linking diagnostic andtreatment system and method for treatment of manifested and latentmaladies using the same by inventors Galloway, et al., filed Jul. 22,2003 and published May 6, 2004, is directed to a computerized meridianlinking diagnostic and treatment system that offers a new paradigm forpractitioners in the EAV, GSR, EDS, and Meridian Stress Assessmentfields. During the entire procedure, the present invention systemoutputs two permanent filters (frequencies) that link all of the body'smeridians and stabilizes the data access points used for testing andcarrying out the many functions of the present invention. The result isan interconnected meridian network linking the internal body systems tothe data access points utilized by the system. The process begins bytaking energetic readings at data access points. The computer stores thepoints that are the most stable. After the stable points are obtained,customized filters (frequencies) relating to specific issues or maladies(such as chemical toxins, allergies, digestion, etc.) are output orbroadcast. Using only a single, but stable data access point as areference point, if any of these filters creates a disturbance to anyenergetic component, cellular component, tissue, organ, or system of thebody, each of which are linked by the interconnected meridian network,an imbalanced reading on the previously stable data access point will becreated. The system will then automatically load products (remedies)that are useful for restoring homeostasis or balance. Each of theremedies are stored in the system database and can easily and quickly bescanned through until one or more products or remedies are discoveredthat will remove the underlying disturbance and allow the patient toobtain an improved level of health. The product/remedy is then placed ina holding tank that stores the results of each test. Specifically, theholding tank stores the filter(s) that created an imbalance/disturbance,the products (remedies) that allow the individual's body to restorehomeostasis, balance, or improved health, and various prescriptionconstraints that dictate administration of the products to the patient.The present invention also features several computer software functions,along with various methods of diagnosing maladies and treating a patientusing an alternative medicine technique similar to a meridian stressassessment.

U. S. Publication No. 20080077434 for system and method foradministration of on-line healthcare by inventors Man, et al., filedJul. 15, 2005 and published Mar. 27, 2008, is directed to a healthcareadministration system useful for the management of anamnesis and medicalrecords, data analysis, guided diagnosis, medical treatment, andclinical investigation. The novel system comprising: a plurality ofself-sufficient subsystems adapted to record, store, share, clinicallyinvestigate and analyze information by means of a common medicalinformation protocol (CMIP); at least one end-unit device adapted todiagnose and/or treat patients, in communication with a subsystem forcontrolling, monitoring and recording the treatment process and itsoutcome by means of a medical protocol; at least one module adapted fora CMIP. The end-unit device is guided by the CMIP so that anamnesis,diagnosis and targeted treatment is dictated, provided, monitored,recorded and/or clinically investigated. The present invention alsodiscloses a guided method for a healthcare administration system, usefulfor the management of medical records, data analysis, diagnosis, guidedtreatment and medical investigation by means of the medical system asdefined above.

U.S. Pat. No. 7,613,510 for biofeedback device displaying results on acellular phone display by inventors Rentea, et al., filed Dec. 11, 2003and issued Nov. 3, 2009, is directed to biofeedback information measuredat a body part of a user. The information is communicated to a cellulartelephone device and used to produce a display on a display screen ofthe cellular telephone device.

U.S. Pat. No. 7,937,139 for systems and methods of utilizing electricalreadings in the determination of treatment by inventors Horne, et al.,filed Jul. 20, 2004 and issued May 3, 2011, is directed to a system fordetermining treatment options from at least two electrical readings. Theelectrical readings are conductivity measurements of a particular regionon the human body. The system utilizes a correlation algorithm todetermine the diagnosis which can easily be correlated with appropriatetreatments. The correlation algorithm may include the analysis ofmultiple electrical readings in determining the diagnosis. The systemmay also utilize a database of clinical data to further assist indetermining the diagnosis.

U.S. Pat. No. 8,099,159 for methods and devices for analyzing andcomparing physiological parameter measurements by inventor Cook, filedSep. 13, 2006 and issued Jan. 17, 2012, is directed to methods anddevices that are capable of measuring physiological parameters of atleast two contact points and determining whether the measured parametersreflect favorable or unfavorable physiological responses are disclosedherein. Specifically, the present invention encompasses a method thatcan non-invasively monitor physiological parameters of at least twocontact points before and after a stimulus is applied to a subject andcompare the measured parameters to determine whether the physiologicalstate of the subject is favorable or unfavorable.

U.S. Pat. No. 8,131,355 for automated skin electrical resistancemeasurement device and method by inventor Clark, filed Aug. 1, 2007 andissued Mar. 6, 2012, is directed to an automated skin resistancemeasurement device having an applied signal selector for selecting oneor more applied signal forms from an applied signal library, an appliedsignal generator in communication with the applied signal selector forgenerating one or more DC applied signals, each applied signal being inthe form of a selected applied signal form, one or more applied signalapplicators for administering the applied signals to test zones on theskin of a human subject, and one or more applied signal resistancesensors for sensing the resistance of the skin of the subject at thetest zones.

U.S. Pat. No. 8,332,027 for electroacupuncture system and method fordetermining meridian energy balance number by inventor Larsen, filed May12, 2010 and issued Dec. 11, 2012, is directed to an electroacupuncturesystem for measuring and treating meridian energy balance in a patient.The system also includes a processing apparatus connected to theelectrical potential source capable of calculating an overall meridianenergy balance number. The processing apparatus may be programmed tocarry out a method for determining a meridian energy balance number.

U.S. Pat. No. 8,682,425 for electropuncture system by inventors Larsen,et al., filed Jan. 30, 2008 and issued Mar. 25, 2014, is directed to anelectroacupuncture system for measuring and treating meridian energybalance in a patient. The system can include a pressure sensitive probeand return path contact, both of which are connected to an electricalpotential source. The probe and contact are meant to be applied to apatient to diagnose and treat meridian energy imbalances. The systemalso includes a processing apparatus connected to the electricalpotential source capable of interpreting the readings taken by theelectrical potential source and probe and affecting operation of thesystem based on the readings. The processing apparatus may also usemeasurements to calculate an overall meridian energy balance number.

U. S. Publication No. 20150230726 for comprehensive health assessmenttool for identifying acquired errors of metabolism by inventor Greaves,filed May 14, 2014 and published Aug. 20, 2015, is directed to a methodof comprehensive health assessment includes using a biocommunication orbioenergetic device to measure signals sent across or through the body.Fluctuations in galvanic skin response are measured and transmitted to acomputer or computing device and compared to a library of possiblestimulus sources, each associated with a predetermined electricalsignature.

U. S. Publication No. 20180042813 for smart equipment with bidirectionaldiagnosis and therapy device by inventor Chiang, filed Aug. 15, 2015 andpublished Feb. 15, 2018, is directed to a smart equipment withbidirectional diagnosis and therapy device, comprising a power supplyunit used for providing each unit with required power, a high-voltagediagnosis and therapy unit provided for diagnosis and therapy as well aselectronic acupuncture and sending back a diagnosis and therapy signal,an input and display unit provided for inputting operation commands anddisplaying related image, a wireless transmission unit provided forconnecting to a cloud database wirelessly, a magnetic disk installedwith program being loaded with application software for processing thediagnosis and therapy signal correspondingly, and a microprocessor usedfor processing related operation. Thereby, the present invention enablesthe user to manipulate the high-voltage diagnosis and therapy unit fordiagnosis and therapy via the input and display unit according tosuggestion from application software. Thus, correct diagnosis andtherapy is allowed for the user to achieve the best effect.

SUMMARY OF THE INVENTION

The present invention relates to devices, methods, and systems formeasuring galvanic skin response based on exposure to stimuli includingelectromagnetic waves and mechanical waves as well as substances exposedto electromagnetic waves and mechanical waves.

It is an object of this invention to provide intelligent analytics andactionable data based on galvanic skin response measurements obtainedduring exposure to stimuli including electromagnetic waves andmechanical waves and substances exposed to electromagnetic waves andmechanical waves.

In one embodiment, the present invention is directed to a system formeasuring galvanic skin response, including an electrical conductivitymeter electrically connected to a positive electrode and a negativeelectrode; and a server platform in network communication with theelectrical conductivity meter; wherein the electrical conductivity meterincludes at least one processor and at least one memory; wherein thenegative electrode is in contact with a first portion of a subject andwherein the positive electrode is in contact with a second portion of asubject, thereby creating a circuit including the positive electrode,the negative electrode, and the subject; wherein the positive electrodeincludes a pressure sensor operable to indicate an amount of pressureapplied by a tip of the positive electrode on the point; wherein theserver platform includes a reasoning engine; and wherein the reasoningengine is operable to detect variations in the pressure applied by thepositive electrode.

In another embodiment, the present invention is directed to a system formeasuring galvanic skin response, including an electrical conductivitymeter electrically connected to a positive electrode and a negativeelectrode; and a server platform in network communication with theelectrical conductivity meter; wherein the electrical conductivity meterincludes at least one processor, at least one memory, a display screen,and a test plate operable to receive at least one element exposed toelectromagnetic waves and/or mechanical waves; wherein the negativeelectrode is in contact with a first portion of a subject and whereinthe positive electrode is in contact with a second portion of a subject,thereby creating a circuit including the positive electrode, thenegative electrode, and the subject; wherein the circuit furtherincludes the at least one element exposed to the electromagnetic wavesand/or the mechanical waves in contact with the test plate; and whereinthe server platform is operable to calculate a compatibility score forthe at least one element exposed to the electromagnetic waves and/or themechanical waves and the subject based on a galvanic skin measurement ofthe subject when the at least one element exposed to the electromagneticwaves and/or the mechanical waves is in contact with the test plate andthereby included in the circuit and a galvanic skin measurement of thesubject when the at least one element exposed to the electromagneticwaves and/or the mechanical waves is not in contact with the test plateand thereby not included in the circuit, wherein the compatibility scoreindicates a degree of effectiveness, a degree of sensitivity, a degreeof tolerance, and/or a tendency to toxicity of the at least one elementexposed to the electromagnetic waves and/or the mechanical waves for thesubject.

In yet another embodiment, the present invention is directed to a systemfor measuring galvanic skin response, including an electricalconductivity meter electrically connected to a positive electrode and anegative electrode; a server platform in network communication with theelectrical conductivity meter; and a device including a photon sourceand/or a Tesla coil operable to emit electromagnetic waves; wherein theelectrical conductivity meter includes at least one processor, at leastone memory, a display screen, and a test plate operable to receive atleast one element exposed to electromagnetic waves and/or mechanicalwaves; wherein the negative electrode is in contact with a first portionof a subject and wherein the positive electrode is in contact with asecond portion of a subject, thereby creating a circuit including thepositive electrode, the negative electrode, and the subject; wherein thecircuit further includes the at least one element exposed to theelectromagnetic waves and/or the mechanical waves in contact with thetest plate; wherein the server platform is operable to calculate acompatibility score for the at least one element exposed to theelectromagnetic waves and/or the mechanical waves and the subject basedon a galvanic skin measurement of the subject when the at least oneelement exposed to the electromagnetic waves and/or the mechanical wavesis in contact with the test plate and a galvanic skin measurement of thesubject when the at least one element exposed to the electromagneticwaves and/or the mechanical waves is not in contact with the test plate,wherein the compatibility score indicates a degree of effectiveness, adegree of sensitivity, a degree of tolerance, and/or a tendency totoxicity of the at least one element exposed to the electromagneticwaves and/or the mechanical waves for the subject; wherein the deviceincluding the photon source and/or the Tesla coil is configured toexpose the at least one element to the electromagnetic waves; andwherein the at least one element includes food, a food component, acoloring, an additive, a preservative, a thickener, a stabilizer, anemulsifier, an enhancer, a beverage, a supplement, a medication, a drug,an herb, a spice, a vitamin, a mineral, a gemstone, a metal, anelectronic device, a bodily fluid, a tissue, and/or a hair sample.

These and other aspects of the present invention will become apparent tothose skilled in the art after a reading of the following description ofthe preferred embodiment when considered with the drawings, as theysupport the claimed invention.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 illustrates one embodiment of an EAV device.

FIG. 2 illustrates another embodiment of an EAV device.

FIG. 3A illustrates a conductivity reading of a balanced meridian.

FIG. 3B illustrates a conductivity reading of an irritated or inflamedmeridian.

FIG. 3C illustrates a degenerated or impaired meridian.

FIG. 4 illustrates a circuit created between a subject and an EAV deviceaccording to one embodiment of the present invention.

FIG. 5 is a flow chart detailing a method of calibrating and testingusing the EAV device according to one embodiment of the presentinvention.

FIG. 6A illustrates a first side of a band electrode according to oneembodiment of the present invention.

FIG. 6B illustrates a second side of the band electrode in FIG. 6A.

FIG. 6C illustrates a patch electrode according to one embodiment of thepresent invention.

FIG. 7A is a diagram of a server platform in network communication withan EAV device via a computing device according to one embodiment of thepresent invention.

FIG. 7B is a diagram of a server platform in network communication withan EAV device via a computing device according to one embodiment of thepresent invention.

FIG. 8 is a diagram of a server platform in network communication with acomputing device configured as a smart EAV device according to oneembodiment of the present invention.

FIG. 9 is a flow chart detailing a method of logging into the serverplatform and updating subject information according to one embodiment ofthe present invention.

FIG. 10 is a schematic diagram of a cloud-based system of the presentinvention according to one embodiment of the present invention.

DETAILED DESCRIPTION

The present invention is generally directed to galvanic skin responsemeasurements and analytics.

In one embodiment, the present invention is directed to a system formeasuring galvanic skin response, including an electrical conductivitymeter electrically connected to a positive electrode and a negativeelectrode; and a server platform in network communication with theelectrical conductivity meter; wherein the electrical conductivity meterincludes at least one processor and at least one memory; wherein thenegative electrode is in contact with a first portion of a subject andwherein the positive electrode is in contact with a second portion of asubject, thereby creating a circuit including the positive electrode,the negative electrode, and the subject; wherein the positive electrodeincludes a pressure sensor operable to indicate an amount of pressureapplied by a tip of the positive electrode on the point; wherein theserver platform includes a reasoning engine; and wherein the reasoningengine is operable to detect variations in the pressure applied by thepositive electrode.

In another embodiment, the present invention is directed to a system formeasuring galvanic skin response, including an electrical conductivitymeter electrically connected to a positive electrode and a negativeelectrode; and a server platform in network communication with theelectrical conductivity meter; wherein the electrical conductivity meterincludes at least one processor, at least one memory, a display screen,and a test plate operable to receive at least one element exposed toelectromagnetic waves and/or mechanical waves; wherein the negativeelectrode is in contact with a first portion of a subject and whereinthe positive electrode is in contact with a second portion of a subject,thereby creating a circuit including the positive electrode, thenegative electrode, and the subject; wherein the circuit furtherincludes the at least one element exposed to the electromagnetic wavesand/or the mechanical waves in contact with the test plate; and whereinthe server platform is operable to calculate a compatibility score forthe at least one element exposed to the electromagnetic waves and/or themechanical waves and the subject based on a galvanic skin measurement ofthe subject when the at least one element exposed to the electromagneticwaves and/or the mechanical waves is in contact with the test plate andthereby included in the circuit and a galvanic skin measurement of thesubject when the at least one element exposed to the electromagneticwaves and/or the mechanical waves is not in contact with the test plateand thereby not included in the circuit, wherein the compatibility scoreindicates a degree of effectiveness, a degree of sensitivity, a degreeof tolerance, and/or a tendency to toxicity of the at least one elementexposed to the electromagnetic waves and/or the mechanical waves for thesubject.

In yet another embodiment, the present invention is directed to a systemfor measuring galvanic skin response, including an electricalconductivity meter electrically connected to a positive electrode and anegative electrode; a server platform in network communication with theelectrical conductivity meter; and a device including a photon sourceand/or a Tesla coil operable to emit electromagnetic waves; wherein theelectrical conductivity meter includes at least one processor, at leastone memory, a display screen, and a test plate operable to receive atleast one element exposed to electromagnetic waves and/or mechanicalwaves; wherein the negative electrode is in contact with a first portionof a subject and wherein the positive electrode is in contact with asecond portion of a subject, thereby creating a circuit including thepositive electrode, the negative electrode, and the subject; wherein thecircuit further includes the at least one element exposed to theelectromagnetic waves and/or the mechanical waves in contact with thetest plate; wherein the server platform is operable to calculate acompatibility score for the at least one element exposed to theelectromagnetic waves and/or the mechanical waves and the subject basedon a galvanic skin measurement of the subject when the at least oneelement exposed to the electromagnetic waves and/or the mechanical wavesis in contact with the test plate and a galvanic skin measurement of thesubject when the at least one element exposed to the electromagneticwaves and/or the mechanical waves is not in contact with the test plate,wherein the compatibility score indicates a degree of effectiveness, adegree of sensitivity, a degree of tolerance, and/or a tendency totoxicity of the at least one element exposed to the electromagneticwaves and/or the mechanical waves for the subject; wherein the deviceincluding the photon source and/or the Tesla coil is configured toexpose the at least one element to the electromagnetic waves; andwherein the at least one element includes food, a food component, acoloring, an additive, a preservative, a thickener, a stabilizer, anemulsifier, an enhancer, a beverage, a supplement, a medication, a drug,an herb, a spice, a vitamin, a mineral, a gemstone, a metal, anelectronic device, a bodily fluid, a tissue, and/or a hair sample.

Referring now to the drawings in general, the illustrations are for thepurpose of describing one or more preferred embodiments of the inventionand are not intended to limit the invention thereto.

Electromagnetic waves and mechanical waves are two prominent methods ofenergy transfer. Generally, electromagnetic waves are emitted byaccelerating electrically charged particles. When an electromagneticwave contacts matter, the electromagnetic wave exerts force on thatmatter, and is capable of imparting energy, momentum, and angularmomentum to that matter. Examples of electromagnetic waves include radiowaves, microwaves, infrared, visible light, ultraviolet (UV) light,X-rays, and gamma rays. In contrast, mechanical waves are an oscillationof matter which transfers energy through a medium. Examples ofmechanical waves include sound waves, seismic waves, and ocean waves.

Accordingly, both electromagnetic and mechanical waves are capable oftransforming the structure of a substance. The structure of liquids suchas water is transformed in nature through light from the sun, naturalelectrical discharges such as lightning, and other natural processes. Itis also possible to produce structured or hexagonal water, as well as tochange the structure of water through purification as described in U.S.Pat. No. 7,793,788 titled “Separating components of aqueous mixtures,suspensions, and solutions”, which is incorporated herein by referencein its entirety. Similarly, magnetic fields, electric fields, andelectromagnetic fields are capable of transforming the structure of asubstance.

Several methods of exposing substances to mechanical waves andelectromagnetic waves are known in the art. QUINT DRINK by QUINTSYSTEMEexposes a liquid such as water to vibrations, thereby transferringenergy to the liquid and altering the structure of the liquid.Similarly, the ULTRACOMPAKT BIOENERGETISCHER STIMULATOR (UBS) 315 byDieter Jossner utilizes microelectronics, LEDs, and a magnetic field totransfer energy to substances and alter the structure of the substances.Specifically, the UBS 315 is capable of producing photons in the form ofwhite light and red light, which is modulated with solar noise.Additionally, the UBS 315 includes an audio socket which provides formodulating the photons and the magnetic field with audio. The magneticfield of the UBS 315 is a scalar magnetic field produced by a Teslacoil. Advantageously, the UBS 315 is operable to alter the structure ofboth liquids and solids. Similarly, Dieter Jossner's AQA 707 providesfor treating water and other liquids with light including the frequencyspectrum of the sun, magnetic fields, energetic fields, and through avortex effect.

Recent research has also shown that exposure to biometric sounds isbeneficial. For example, a paper titled “Mother's voice and heartbeatsounds elicit auditory plasticity in the human brain before fullgestation” by Alexandra R. Webb, Howard T. Heller, Carol B. Benson, andAmir Lahav (published in Proceedings of the National Academy of Sciencesof the United States of America on Mar. 10, 2015) demonstrated thatnewborns who were exposed to audio recordings of maternal soundsincluding their mother's voice and their mother's heartbeat developed asignificantly larger auditory cortex compared to newborns who were notexposed to such auditory recordings. Similarly, Stanford University hasbeen granted U.S. Pat. No. 9,888,884 titled “Method of sonifying signalsobtained from a living subject”, which describes providing aural signalsbased on a subject's heart or brain to the subject as biofeedback. Thebiofeedback includes neurotherapy, which is utilized as a therapy formigraines, autism, attention deficit hyperactivity disorder (ADHD),and/or cognitive performance.

What is needed are systems and methods for quantitatively measuring asubject's reaction to electromagnetic and mechanical waves andcompatibility with electromagnetic and mechanical waves, as well as asubject's reaction to and compatibility with substances exposed toelectromagnetic and mechanical waves. In particular, none of the priorart discloses quantitatively measuring a subject's reaction to lightand/or sound constructed based on measurable biological outputs orsubstances exposed to light and/or sound constructed based on measurablebiological outputs.

One embodiment of the present invention includes measuring, recording,or otherwise obtaining biological outputs and/or biometric sounds from asubject or a living being of interest. Biological outputs include, byway of example and not limitation, heartbeats, brainwaves, neuraloscillations, breathing patterns, and/or combinations thereof.Alternatively, resonance frequencies of a subject or a living being ofinterest including resonance frequencies of organs, bones, tissue,and/or cartilage. By way of example the resonance frequencies of aspinal column, a head, a chest wall, an abdomen, shoulders, lungs, legs,arms, hands, feet, an ocular globe, and/or a maxilla are measured andrecorded as vibrations and/or sound waves. In another embodiment,resonance frequencies of an object, or natural occurrences such aslightning, the ionosphere of a planet, etc. are measured and recorded asvibrations and/or sound waves. Biometric sounds include speech (e.g.,mother's voice). The biological outputs' resonance frequencies, orbiometric sounds are recorded using a digital recorder or an analogrecorder. Alternatively, the biological outputs, resonance frequencies,or biometric sounds are measured by a particular machine such as anelectroencephalography (EEG) machine, an electrocardiography (ECG)machine, or a machine that measures resonance frequencies such as the353B34 PCB accelerometer by PCB PIEZOTRONICS or the ULTRALIGN G2 bySIGMA INSTRUMENTS.

The living being of interest includes a living being known to thesubject or related to the subject, by way of example and not limitation,a subject, a member of a subject's family such as a spouse, father,mother, child, grandchild, brother, sister, cousin, aunt, uncle,grandfather, grandmother, etc., a significant other, a friend, or a petsuch as a dog or a cat. Alternatively, the living being of interestincludes a living being not personally known to the subject, such as anathlete, celebrity, or a living being with certain qualities such asphysical qualities, emotional qualities, spiritual qualities, mentalqualities, etc. Alternatively, the living being of interest includes ananimal, a mammal, a reptile, amphibian, fish, bird, bacteria, virus,plant, etc. In one embodiment of the present invention, the term animalincludes a human. In another embodiment of the present invention, theterm animal does not include a human. In another embodiment, the livingbeing of interest was previously living and is now deceased.

Resonance frequencies of objects in one embodiment include resonancefrequencies of objects with significance to a living being of interest,such as an object from childhood, an object of a family member orfriend, an object associated with a professional or personalachievement, etc.

In one embodiment, the resonance frequencies and/or biological outputsare recorded as a mechanical wave such as a sound or a vibration. Therecording is preferably digital, but is an analog recording in anotherembodiment. Sounds are recorded via any method known to one skilled inthe art, such as via a microphone connected to a recorder operable torecord to a magnetic tape device or a microphone connected to anelectronic device such as a laptop, tablet, smart phone, etc. running anapplication program. Vibrations are recorded utilizing a vibration datalogger, a vibration meter, and/or any other apparatus known in the artfor recording vibrations. Once recorded, the sounds and/or vibrationsare operable to be combined to produce a combined sound or vibration.

In another embodiment, a sound and/or vibration is converted ortranslated into electromagnetic waves such as visible light. SOUND OFSOUL by AQUAQUINTA (Austria) provides for translation of heart ratevariability (HRV) into sound and/or colored light. Additionally, US Pub.No. 2017/0007847 titled “Bioresonance frequency emitting device, system,and method” which is incorporated herein by reference in its entirety,provides one or more LEDs which emit light at a certain intensity,frequency, or flicker-rate based on one or more bioresonances. Thepresent invention provides for translation of any mechanical wave and/orelectromagnetic wave or groups of mechanical waves and/orelectromagnetic waves into another mechanical wave and/orelectromagnetic wave and/or groups of other mechanical waves and/orelectromagnetic waves. In one example, music is converted into light ora sound vibration. In another example, a sound and/or vibration isconverted or translated into an audio file such as a musical track, abinaural beat track, a track of a natural sound such as ocean waves orwildlife, or a track of someone speaking. U.S. Pat. No. 9,888,884, whichis incorporated herein by reference in its entirety, describesdetermining the beats per minute (BPM) of biometric data and translatingthe BPM into rhythmic content such as music. Similarly, the BPM of thesound and/or vibration is operable to be converted into rhythmic contentin the present application. Alternatively, the BPM of the sound and/orvibration is operable to be matched against a database of music formatches to the sound and/or vibration. Music and musical tracks includetonal and atonal music and music from any genre such as electronic,rock, soul, R&B, hip-hop, reggae, folk, country, classical, jazz,avant-garde, and all sub-genres thereof.

In another embodiment, the present invention provides for a device orsystem exposing a substance to electromagnetic and/or mechanical waves.Exposure to the electromagnetic and/or mechanical waves alters thestructure of the substance. In one embodiment, this exposure isperformed with the ULTRACOMPAKT BIOENERGETISCHER STIMULATOR (UBS) 315 oranother device with photon sources and/or a Tesla coil. The photonsource of the device preferably emits red and white photons.Additionally, the Tesla coil preferably has a 40% scalar content with anapproximate field strength of 150 μT. Alternatively, a device isoperable to create magnetic, electric, and/or electromagnetic fieldsthrough a combination of magnets, electromagnets, and/or coils.

In another alternative, a substance is exposed to mechanical waves suchas the waves in an ocean or a lake. The substance is exposed directly inone embodiment, but alternatively is placed in a container and exposedto the waves.

The present invention also provides for exposing a substance to one ormore volatile chemical compounds or odors which alter the structure ofthe substance. Alternatively, the volatile chemical compounds or odorsare translated into a digital signal. One method of translating thevolatile chemical compounds or odors into digital signals is describedin WIPO Pub. No. WO2019040910A1, which is incorporated herein byreference in its entirety.

The substance exposed includes any liquid, solid, and/or gas. Examplesof common substances include a food, a food component (e.g., coloring,additive, preservative, thickener, stabilizer, emulsifier, enhancer), abeverage, a supplement, a medication, a drug, an herb, a spice, avitamin, a mineral, a gemstone, a metal, an electronic device, a bodilyfluid, a tissue, and/or a hair sample.

As previously discussed, Dr. Reinhard Voll, a German physician andengineer, developed a method of measuring galvanic skin response knownas Electroacupuncture According to Voll (EAV) in the 1940s. EAV is oneapplication of measuring galvanic skin response. EAV utilizes principlesof acupuncture based on meridians. EAV differs from traditional Chineseacupuncture in that there are 21 basic EAV meridians instead of 12principal meridians. Acupuncture points on these meridians correspond toglands, internal organs, and/or subcomponents of internal organs.Electrical conductivity of the skin is higher on acupuncture points thanon other locations. Dr. Helmut Schimmel improved EAV in the 1970s byutilizing a single acupuncture point instead of multiple points.

An electrical conductivity meter is used to measure galvanic skinresponse. An EAV device is one type of electrical conductivity meter. Apractitioner tests a meridian point with a probe that corresponds to apositive electrode. The positive electrode is preferably a stylus with abrass or silver tip. A subject contacts (e.g., holds) a negativeelectrode. The practitioner tests the conductivity of a plurality ofmeridian points by contacting the skin of the subject with the positiveelectrode at a specific meridian point on the hands or feet. Thenegative electrode and positive electrode are electrically connected tothe EAV device (e.g., via cables). A small amount of current travelsthrough the body when the positive electrode contacts the skin.

FIG. 1 illustrates one embodiment of an EAV device. The EAV device 100is electrically connected to a probe 102 (i.e., positive electrode) anda negative electrode 104. A meter 106 displays a conductivity readingbetween 0 and 100. A test plate 108 is used to test at least oneelement. A power button 110 is used to turn the EAV device 100 on oroff. A power cord 112 connects the EAV device 100 to alternating current(AC) power. Alternatively, the EAV device is powered by at least onebattery (e.g., rechargeable battery). A foot pedal 114 is optionallyused to toggle between menu items displayed on a screen 116. In oneembodiment, the screen is a touch screen. The EAV device 100 isconnected via a wired connection or a wireless connection to a computingdevice 118. The EAV device 100 preferably has a pressure range indicator120 to indicate a pressure exerted by the tip of the probe 102 on asurface (e.g., skin). Manuals for the Vega® BIO-expert and the Wegamed™Test Expert Plus include additional details regarding EAV devices, eachof which is incorporated herein by reference in its entirety. Additionalinformation regarding testing is included in the “Short Manual of theVEGATEST-method” by Fehrenbach et al., including both the 2^(nd) ed.(1986) and SKU no. FLIT0.13059, available athttps://www.wegamed.de/product/short-manual-of-the-vegatest-method-2/,each of which is incorporated herein by reference in its entirety.

The probe preferably includes a pressure sensor to indicate an amount ofpressure exerted by the tip of the probe on a surface. In anotherembodiment, the probe includes a three-dimensional (3D) accelerometer tomeasure a position (e.g., angle) of the probe. Alternatively oradditionally, the probe includes a 3D gyroscope to measure a position orangle of the probe.

The EAV device preferably includes at least one processor. By way ofexample, and not limitation, the at least one processor is ageneral-purpose microprocessor (e.g., a central processing unit (CPU)),a graphics processing unit (GPU), a microcontroller, a Digital SignalProcessor (DSP), an Application Specific Integrated Circuit (ASIC), aField Programmable Gate Array (FPGA), a Programmable Logic Device (PLD),a controller, a state machine, gated or transistor logic, discretehardware components, or any other suitable entity or combinationsthereof operable to perform calculations, process instructions forexecution, and/or otherwise manipulate information. In one embodiment,one or more of the at least one processor is operable to run predefinedprograms stored in at least one memory of the EAV device.

The EAV device preferably includes at least one antenna, which allowsthe EAV device to transmit data to at least one computing device (e.g.,smartphone, tablet, laptop computer, desktop computer). In a preferredembodiment, the EAV device is in wireless network communication with theat least one computing device. The wireless communication is, by way ofexample and not limitation, radio frequency (RF), BLUETOOTH, ZIGBEE,WI-FI, wireless local area networking, near field communication (NFC),or other similar commercially utilized standards. Alternatively, the atleast one computing device is in wired communication with the controlunit through universal serial bus (USB), FireWire®, or equivalent.

FIG. 2 illustrates another embodiment of an EAV device. In thisembodiment, the EAV device 200 is connected via a wired connection(e.g., cable 250) to the computing device 118 (e.g., smartphone, tablet,laptop computer, desktop computer). A power cord 212 connects the EAVdevice 200 to alternating current (AC) power. Alternatively, the EAVdevice is powered by at least one battery (e.g., rechargeable battery).The EAV device 200 is connected to the probe 102 and the negativeelectrode 104. A test plate 208 is selectively added or removed to theEAV device 200 via a test plate cable 252. Advantageously, the EAVdevice 200 provides for greater portability than the EAV device shown inFIG. 1 due to its modular nature and use of at least one processor onthe computing device.

An EAV device uses a voltage of less than 1.5V and a measurement currentof less than 12 μA. In a preferred embodiment, the EAV device uses avoltage of 1.5V and a measurement current of 10 μA. The EAV device iscalibrated to give a conductivity reading of 0 to 100. A balancedmeridian has a conductivity reading of 50 or approximately 50 as shownin FIG. 3A. A conductivity reading greater than 50 or greater thanapproximately 50 (e.g., >55) indicates irritation or inflammation of themeridian as shown in FIG. 3B. Inflamed tissue swells with water, whichresults in a higher electrical conductivity. A conductivity reading lessthan 50 or less than approximately 50 (e.g., <45) indicates degenerationor impairment of the meridian as shown in FIG. 3C. A chronicallyimpaired organ becomes harder and loses hydration, which results in alower electrical conductivity.

FIG. 4 illustrates a circuit created between a subject and an EAVdevice. As previously described, the EAV device 100 is connected to aprobe 102 (i.e., positive electrode) and a negative electrode 104. Theprobe 102 is shown contacting a subject 290 on a first hand. A secondhand of the subject 290 is holding the negative electrode 104. Touchingthe probe 102 to the first hand while the subject 290 holds the negativeelectrode 104 creates a circuit. In another embodiment, the circuit alsoincludes at least one element (e.g., food, beverage, supplement) on thetest plate of the EAV device.

FIG. 5 is a flow chart detailing a method of calibrating and testingusing the EAV device. The method 300 includes a step of calibrating 302the EAV device. The calibration includes setting a noise threshold anddetermining whether signals need to be amplified. After calibration, themethod 300 includes a step 304 of checking a force field of the subject,a step 306 of checking an immune system of the subject, and a step 308of checking an energy level of the subject. Steps 304-308 create abaseline for the reading.

A biological index of the subject is measured in step 310. Thebiological index is preferably a characteristic of the mesenchyme (i.e.,connective tissue). The connective tissue reflects a biological age of asubject. In a preferred embodiment, the biological index includesnumbers between 1 and 21, wherein lower numbers (e.g., 1) correspond toyounger biological age and higher numbers (e.g., 21) correspond tohigher biological age. In another embodiment, a biological index valueof 15 or greater reflects a health problem.

In step 312, it is determined whether there is a problem with thebiological index of the subject (e.g., value>15). If there is not aproblem with the biological index, the method 300 proceeds to step 322.If there is a problem with the biological index, a biological subsystemof a plurality of biological subsystems is checked in step 314. Afterthe measurement of the biological subsystem, it is determined whetherthere is a problem with the biological subsystem (e.g., conductivityreading>55, conductivity reading<45) in step 316. If there is a problemwith the biological subsystem, individual components within thebiological subsystem are checked for problems in step 318. The problemsinclude, but are not limited to, increased acidity, presence of at leastone bacterium, presence of at least one virus, and imbalance of yeast.After all individual components within the biological subsystem arechecked for problems, it is determined in step 320 whether thebiological subsystem tested in step 314 was the final biologicalsubsystem. If there was not a problem with the biological subsystem instep 316, the method 300 proceeds to step 320. If the biologicalsubsystem was not the final biological subsystem, the method 300 returnsto step 314. If the biological subsystem was the final biologicalsystem, at least one element is tested in step 322.

To test reactions to different elements, at least one element is placedin and/or on a test plate to put the at least one element in circuitwith the subject. The test plate is preferably formed of metal. In apreferred embodiment, the test plate includes a plurality of cylindricalholes drilled into the test plate. Each of the plurality of cylindricalholes is operable to hold an ampule or a vial of an element to betested.

The at least one element includes, but is not limited to, a food, a foodcomponent (e.g., coloring, additive, preservative, thickener,stabilizer, emulsifier, enhancer), a beverage, a supplement, amedication, a drug, an herb, a spice, a vitamin, a mineral, a gemstone,a metal, an electronic device, a bodily fluid, a tissue, and/or a hairsample. The test plate allows for one or more of the at least oneelement to be selectively added or selectively removed from the circuit.

In a preferred embodiment, the ampule or the vial containing the atleast one element is labeled to identify its contents. In oneembodiment, the ampule or the vial is labeled with a barcode.Alternatively, the ampule or the vial is labeled with a passive radiofrequency identification (RFID) tag. In one embodiment, a scanner forthe label is connected via a cable (e.g., USB, FireWire®, or equivalent)to the EAV device. Alternatively, the scanner is built into the EAVdevice.

In yet another embodiment, an element library is used to store digitalsignatures of at least one element. An algorithm compares a conductivityreading of a subject when there is no element in the test plate with thedigital signatures of the at least one element to determine whether aresponse to the at least one element is positive, negative, or neutral.Alternatively, a digital signature is incorporated into the testingcircuit. This is accomplished in a variety of ways. In one example, adigital signature is introduced into the testing circuit by softwarerunning on the EAV device and a new conductivity measurement isobtained. Each conductivity measurement is affected by an energetic linkbetween the subject and the digital signature. Advantageously, utilizinga digital signature allows for the at least one element to be testedwithout placing a sample of the at least one element on a test plate.

In another embodiment of the present invention, a conductivity readingof a subject is taken contemporaneously with exposure of the subject toelectromagnetic and/or mechanical waves. The electromagnetic and/ormechanical waves include any electromagnetic and/or mechanical waveindividually or in combination, including sound, vibration, light,music, etc., individually or in combination. The electromagnetic and/ormechanical waves are generated from resonance frequencies and/orbiological outputs in one embodiment. Alternatively, the electromagneticand/or mechanical waves are not generated from resonance frequencies orbiological outputs but are naturally occurring electromagnetic and/ormechanical waves, machine-made electromagnetic and/or mechanical waves,or man-made electromagnetic and/or mechanical waves.

Alternatively, one or more digital signatures of electromagnetic and/ormechanical waves are created and a conductivity reading of the subjectwithout an element in the test plate is compared with the one or moredigital signatures of the electromagnetic and/or mechanical waves. Inanother embodiment, a digital signature is incorporated into the testingcircuit.

In yet another embodiment, a substance is exposed to mechanical wavesand/or electromagnetic waves and placed in the test plate and theconductivity of the subject is measured. In one embodiment, thesubstance is exposed to the mechanical waves and/or electromagneticwaves while in the test plate and the conductivity of the subject ismeasured. One or more digital signatures of substances exposed toelectromagnetic and/or mechanical waves are also operable to be createdand a conductivity reading of the subject without an element in the testplate is compared with the one or more digital signatures of theelectromagnetic and/or mechanical waves.

The present invention also provides for measuring a conductivity readingof a subject contemporaneously with exposure of the subject to one ormore volatile chemical compounds or odors. The one or more volatilechemical compounds or odors are also operable to be included in acontainer on the test plate in gaseous or liquid form. An example ofvolatile chemical compounds includes perfumes. Alternatively, volatilechemical compounds or odors collected from living beings includingpeople, dogs, cats, etc. are collected and a conductivity reading orcompatibility score determines the compatibility of the subject with theliving being. Similar to the embodiments described above, the one ormore volatile chemical compounds or odors are also operable to betranslated into digital representations of the one or more volatilechemical compounds or odors and compared to a subject's conductivityreading or inserted into the test circuit to obtain conductivityreading(s) specific to the one or more volatile chemical compounds orodors.

In one embodiment, an EAV device is in network communication with aserver platform via a computing device. The computing device is in wiredor wireless communication with the EAV device. The computing device isinstalled with at least one application program operable to provide agraphical user interface (GUI) operable for toggling between differentsteps, recording testing data at different steps, and display diagnosticresults and recommended treatment plans.

In one embodiment, the present invention provides a smart EAV device indirect network communication with a server platform. An example of asmart EAV device is shown in FIG. 2 . The smart EAV device comprises acomputing module, a communication module, and a display module. Thecomputing module is operable to collect and process data from a testingcircuit. The communication module is operable to communicate with aserver platform. The display module comprises a GUI. In one embodiment,the smart EAV device is a smartphone, a tablet, a laptop, and/or anyother portable device, installed with an application program in networkcommunication with a server platform.

In one embodiment, the present invention provides a circuit toolkitincluding at least one signal sensor device (e.g., electrodes, bandsembedded with sensors), a testing plate, and an adapter module. Anexample of the circuit toolkit is shown in FIG. 2 . The adapter moduleconnects the testing plate, the two electrodes, and a subject into acircuit, and transmits data signals to the EAV device.

In one embodiment, at least one electrode is configured as a patch or aband wrapping around a finger portion which includes an acupuncturepoint. The patch or the band includes a galvanic skin sensor to contactthe acupuncture point of a subject. In one embodiment, the patch or theband is embedded with a pressure sensor to measure and display thepressure of the band on the finger to make sure the pressure is in anacceptable range. In another embodiment, the patch or the band includesa hydration sensor to measure a level of hydration of the subject.Advantageously, eliminating variability in pressure of the probe and/orthe location of the probe gives more accurate results and moreconsistent results between practitioners. Additionally, using the patchor the band frees a practitioner's hands to run the EAV device and/orthe computing device. In one embodiment, the patch or the band furtherincludes a computing module in communication with the hydration sensor,the pressure sensor, and the galvanic skin sensor. The computing modulecomprises an Artificial Intelligence (AI)-based algorithm to learn thepatterns of the hydration data and automatically calculates the optimalpressure for the galvanic skin sensor so as to obtain accurate testingresults for a subject. Hydration data is alternatively used to normalizeconductivity readings of meridians, as the hydration level of the skinaffects the conductivity of skin. In another embodiment, a moistureand/or salinity sensor in the band electrode measures an amount ofmoisture and/or concentration of sodium in the moisture at the contactpoint between the band electrode and the skin and normalizesconductivity readings based on these measurements.

FIG. 6A illustrates a first side 402 of a band electrode 400 accordingto one embodiment of the present invention. The first side 402 includesa galvanic skin sensor (e.g., probe) 404, a hydration sensor 406, and apressure sensor 408. The first side 402 preferably includes a computingmodule 410 (e.g., microprocessor) and/or an antenna 412. The computingmodule 410 is operable to perform calculations using data from thegalvanic skin sensor 404, the hydration sensor 406, and/or the pressuresensor 408. Alternatively, data from the galvanic skin sensor 404, thehydration sensor 406, and/or the pressure sensor 408 is calculated onthe EAV device and/or the server platform. The antenna 412 is operableto wirelessly transmit (e.g., via BLUETOOTH, NFC, RF, RFID, WI-FI) datato the EAV device and/or the server platform. Alternatively, data fromthe galvanic skin sensor 404, the hydration sensor 406, and/or thepressure sensor 408 is transmitted via a wired connection to the EAVdevice and/or the server platform. The first side 402 also includes hooktape 414.

FIG. 6B illustrates a second side 416 of the band electrode 400 in FIG.6A. The second side 416 includes loop tape 418. In another embodiment,the first side includes loop tape and the second side includes hooktape. Alternatively, the band electrode is secured using an adhesive oran elastic.

FIG. 6C illustrates a patch electrode 420 according to one embodiment ofthe present invention. The patch electrode 420 includes a galvanic skinsensor (e.g., probe) 404, a hydration sensor 406, and a pressure sensor408. The first side 402 preferably includes a computing module 410(e.g., microprocessor) and/or an antenna 412. The computing module 410is operable to perform calculations using data from the galvanic skinsensor 404, the hydration sensor 406, and/or the pressure sensor 408.Alternatively, data from the galvanic skin sensor 404, the hydrationsensor 406, and/or the pressure sensor 408 is calculated on the EAVdevice and/or the server platform. The antenna 412 is operable towirelessly transmit (e.g., via BLUETOOTH, NFC, RFID, WI-FI) data to theEAV device and/or the server platform. Alternatively, data from thegalvanic skin sensor 404, the hydration sensor 406, and/or the pressuresensor 408 is transmitted via a wired connection to the EAV deviceand/or the server platform. The patch electrode 420 includes an adhesive422 for attachment to the skin.

In one embodiment, the application program installed on the smart EAVdevice includes a GUI to facilitate operations, and a computing modulefor data collection and packaging.

In one embodiment, the smart EAV device comprises a camera operable tocapture images of the testing circuit. The server platform is operableto process the captured images based on an AI/machine learning algorithmand detect any defects in the circuit and send warnings and/orsuggestions to the user for correction. In one embodiment, the smart EAVdevice includes an AI-powered virtual assistant to verbally instruct theuser for self-testing. The AI-power virtual assistant understandsnatural language voices, converses with the user, and executes voicecommands.

In one embodiment, the server platform comprises a database storinghistorical data from tested subjects. The database is continuouslyupdated with new obtained data. The historical data includes subjectprofile data, baseline data, diagnostic data and treatment data oftested subjects. The subject profile data includes gender, sex, age,race, and/or medical history (e.g., conditions, medications, nutritionalsupplements, weight, body mass index (BMI)) of a tested subject. Thebaseline data includes force field data, immunity data, energy leveldata, and volume control data for a tested subject pre-treatment andpost-treatment.

In one embodiment, the server platform includes a proprietary organlibrary. In another embodiment, the server platform is operable toaccess a third-party organ library via an Application Program Interface(API).

In one embodiment, the server platform includes a proprietary problemlibrary. The proprietary problem library includes different problemmodels for a specific organ. In one embodiment, problems in a specificorgan include, but are not limited to, increased acidity, presence of atleast one bacterium, presence of at least one virus, and imbalance ofyeast.

In one embodiment, the server platform includes a proprietary elementlibrary. The element library includes biosignature data for differenttypes of food and other elements mentioned before. The server platformis operable to update the element library with new elements introducedto the market. In one embodiment, the server platform comprises amodeling engine operable to build a virtual element based on a machinelearning algorithm. The machine learning algorithm is operable tocontinuously extract data regarding new elements from various databaseand/or data sources. The modeling engine is operable to automaticallybuild a virtual element based on collected data. In another embodiment,the modeling engine is operable to build a virtual element based on datainput by a user via a GUI. In one embodiment, the server platform isoperable to access to a third-party element library via an API.

In one embodiment, the server platform comprises a classification engineoperable to classify the historical data and incoming data from testedsubjects. The classification is based on gender, age range, race,organs, etc.

In one embodiment, the server platform comprises a reasoning enginebuilt with artificial intelligence (AI) algorithms. The reasoning engineis operable to generate a reasoning model based on multiple sets oftraining data. The multiple sets of training data are a subset ofhistorical data. For example, a subject's health condition issignificantly improved after a specific treatment for a predeterminedperiod of time. The training data includes context data (e.g., baselinedata, testing data) and action data (e.g., treatment data). Thereasoning model is updated periodically when there is an anomalyindicated in the action data produced by the reasoning data based on thecontext data. Each of U.S. Pat. No. 9,922,286 titled “Detecting andCorrecting Anomalies in Computer-Based Reasoning Systems” and U.S.application Ser. No. 15/900,398 is incorporated herein by reference inits entirety.

In another embodiment, the AI algorithms are operable to detectvariations in pressure applied by a practitioner during a session andacross multiple sessions (e.g., single subject with multiple sessions,multiple subjects). In yet another embodiment, the AI algorithms areoperable to detect variations in an angle of the probe. Pressure appliedby the practitioner and the angle of the probe can both affect theconductivity readings. Advantageously, this allows the AI algorithms todetect and address bias both within a session for a single subject andover time with multiple subjects. For example, the AI algorithms areoperable to detect if the practitioner tends to lower the angle of theprobe towards the end of sessions for all subjects, indicating that thepractitioner is fatigued and/or not focused after 45 minutes.Additionally, AI algorithms are operable to address differences inhydration determined via a hydration sensor of a single subject within asingle session or for a single subject or multiple subjects overmultiple sessions. In another embodiment, AI algorithms detect andaccount for differences in moisture or salinity at the contact pointbetween the band electrode and the skin of a single subject over onesession or multiple sessions or for multiple subjects over multiplesessions.

In one embodiment, the reasoning model is operable to generate atreatment plan for a subject based on the test results. The test resultsinclude organ reports and element test reports. The organ reportsinclude conductivity readings for organs and identified problems fororgans with conductivity readings greater than 50. The element testreports include conductivity readings and biometric index scorescorresponding to different types of elements (e.g., food, foodcomponent, beverage, supplement, medication, drug, herb, spice, vitamin,mineral, gemstone, metal, electronic device, bodily fluid, tissue, hairsample).

In one embodiment, the server platform comprises an optimization engineto optimize an overall treatment plan for a subject to get maximumeffectiveness when more than one problem organ is detected so that thetreatment plan is good for all the problem organs, or at least certaintreatments good for one problem organ do not worsen other problemorgans.

FIG. 7A is a diagram of a server platform 502 in network communicationwith an EAV device 100 via a computing device 118 according to oneembodiment of the present invention. The server 502 incudes a historicaldatabase 504, a proprietary library 506, a user library 508, a modelingengine 510, a classification engine 512, a reasoning engine 514, and anoptimization engine 516. The computing device 118 includes a GUI 518.

FIG. 7B is a diagram of a server platform 502 in network communicationwith an EAV device 100 via a computing device 118 according to anotherembodiment of the present invention. FIG. 7B differs from FIG. 7A inthat the proprietary library 506 is on the EAV device 100 rather than onthe server 502.

FIG. 8 is a diagram of a server platform 502 in network communicationwith a computing device configured as a smart EAV device 200 accordingto one embodiment of the present invention. The server 502 incudes ahistorical database 504, an organ library 520, a problem library 522, anelement library 524, a modeling engine 510, a classification engine 512,a reasoning engine 514, and an optimization engine 516.

In one embodiment, the server platform is operable to automatically scaneach subsystem of a subject based on the organ library and generate anorgan report for the subject. The organ report includes conductivityreadings for all organs. Problem organs are identified with conductivityreadings larger than a threshold. In one embodiment, the threshold is50, 55, 60, 65, or 70. Potential problems are identified for the problemorgans as well. The server platform is also operable to automaticallytest a category of elements based on the element library and generate anelement test report. The element test report comprises conductivityreadings and biometric index scores corresponding to the test elements,comparing to the baseline conductivity reading and baseline biometricindex score of the subject.

In one embodiment, the server platform is operable to generate atreatment report based on the organ report and the element test reportof a subject. The treatment report includes elements good for thesubject and elements to be avoided and/or limited by the subject.

In another embodiment, the server platform is operable to generate aprogress report. The progress report displays historical changes in theorgan report and/or the element test report over time.

In one embodiment, the server platform provides licensed access via API.An application program is downloaded and installed on a computingdevice. A user account is created based on the type of the user (e.g.,enterprise, practitioner, and individuals). User identification isrequired for performing tests and accessing to historical data of theuser. In one embodiment, biometric data is used for user authentication,for example, facial features, fingerprints, voices, heartbeats, veinrecognition, etc. In another embodiment, a password is used for userauthentication.

FIG. 9 is a flow chart detailing a method 600 of logging into the serverplatform and updating subject information. The user logs into the serverplatform in step 602. It is determined whether the subject is a newsubject in step 604. If the subject is a new subject, the new subject isadded to the database in step 606. A history for the new subject isadded to the database in step 608 and the user begins calibration instep 614. If the subject is not a new subject, it is determined whetherthere are changes to a history for the subject in step 610. If there arechanges to the history for the subject, the history is updated in step612 before the user begins calibration in step 614. If there are notchanges to the history in step 610, the user begins calibration in step614.

The server platform is preferably operable to automatically transmit atleast one report to the subject. Additionally, the server platform isoperable to bill the subject and create appointments.

In one embodiment, the application program installed on a mobile deviceis operable to calculate a compatibility score of an element, anelectromagnetic wave, a mechanical wave, an odor including one or morevolatized chemical compounds, and combinations thereof for a specificuser based on historical data stored. In one embodiment, thecompatibility score indicates a degree of effectiveness, a degree ofsensitivity, a degree of tolerance, and/or a tendency to toxicity forthe specific user, each of which is in a range between 0 and 4. In oneexample, wild salmon is given a degree of effectiveness of 4 and farmedsalmon is given a degree of effectiveness of 2 because the ratio ofOmega-3:Omega-6 is higher in wild salmon than farmed salmon. In anotherexample, food sensitives are given a range between 0 and 4, wherein 0indicates no food sensitivity, 1 indicates a food sensitivity, and 4indicates highly allergic. In one embodiment, the score is in a rangebetween −7 and 17 by weighing the effectiveness, sensitivity, tolerance,and toxicity. In another embodiment, the score is in a range between −7and 19. In yet another embodiment, the score is in a range between −10and 20. The higher the score is, the better it is for the specific user.Negative scores indicate potential damage and/or threats to a specificuser. For example, pain relievers harm the kidneys, even though they areeffective to reduce pain. In one example, a toxic element is given ascore of −2, an average remedy is given a score of between 4 and 7, andan excellent remedy is given a score of between 10 and 19. Theapplication program is operable to recognize the elements with a barcodescan or through image recognition via the mobile device.

In one embodiment, the server platform provides training programs forusers. A user accesses the training programs by logging in to theiraccount. In one embodiment, the training program is a pre-recordeddemonstration or tutorial. In another embodiment, the training programis AI-powered and operable to verbally instruct a user for a testingstep by step. The training program provides test reproducibility andenables mass adoption.

FIG. 10 is a schematic diagram of an embodiment of the inventionillustrating a computer system, generally described as 800, having anetwork 810, a plurality of computing devices 820, 830, 840, a server850, and a database 870.

The server 850 is constructed, configured, and coupled to enablecommunication over a network 810 with a plurality of computing devices820, 830, 840. The server 850 includes a processing unit 851 with anoperating system 852. The operating system 852 enables the server 850 tocommunicate through network 810 with the remote, distributed userdevices. Database 870 may house an operating system 872, memory 874, andprograms 876.

In one embodiment of the invention, the system 800 includes acloud-based network 810 for distributed communication via a wirelesscommunication antenna 812 and processing by at least one mobilecommunication computing device 830. Alternatively, wireless and wiredcommunication and connectivity between devices and components describedherein include wireless network communication such as WI-FI, WORLDWIDEINTEROPERABILITY FOR MICROWAVE ACCESS (WIMAX), Radio Frequency (RF)communication including RF identification (RFID), NEAR FIELDCOMMUNICATION (NFC), BLUETOOTH including BLUETOOTH LOW ENERGY (BLE),ZIGBEE, Infrared (IR) communication, cellular communication, satellitecommunication, Universal Serial Bus (USB), Ethernet communications,communication via fiber-optic cables, coaxial cables, twisted paircables, and/or any other type of wireless or wired communication. Inanother embodiment of the invention, the system 800 is a virtualizedcomputing system capable of executing any or all aspects of softwareand/or application components presented herein on the computing devices820, 830, 840. In certain aspects, the computer system 800 may beimplemented using hardware or a combination of software and hardware,either in a dedicated computing device, or integrated into anotherentity, or distributed across multiple entities or computing devices.

By way of example, and not limitation, the computing devices 820, 830,840 are intended to represent various forms of digital computers 820,840, 850 and mobile devices 830, such as a server, blade server,mainframe, mobile phone, personal digital assistant (PDA), smartphone,desktop computer, netbook computer, tablet computer, workstation,laptop, and other similar computing devices. The components shown here,their connections and relationships, and their functions, are meant tobe exemplary only, and are not meant to limit implementations of theinvention described and/or claimed in this document

In one embodiment, the computing device 820 includes components such asa processor 860, a system memory 862 having a random access memory (RAM)864 and a read-only memory (ROM) 866, and a system bus 868 that couplesthe memory 862 to the processor 860. In another embodiment, thecomputing device 830 may additionally include components such as astorage device 890 for storing the operating system 892 and one or moreapplication programs 894, a network interface unit 896, and/or aninput/output controller 898. Each of the components may be coupled toeach other through at least one bus 868. The input/output controller 898may receive and process input from, or provide output to, a number ofother devices 899, including, but not limited to, alphanumeric inputdevices, mice, electronic styluses, display units, touch screens, signalgeneration devices (e.g., speakers), or printers.

By way of example, and not limitation, the processor 860 may be ageneral-purpose microprocessor (e.g., a central processing unit (CPU)),a graphics processing unit (GPU), a microcontroller, a Digital SignalProcessor (DSP), an Application Specific Integrated Circuit (ASIC), aField Programmable Gate Array (FPGA), a Programmable Logic Device (PLD),a controller, a state machine, gated or transistor logic, discretehardware components, or any other suitable entity or combinationsthereof that can perform calculations, process instructions forexecution, and/or other manipulations of information.

In another implementation, shown as 840 in FIG. 10 , multiple processors860 and/or multiple buses 868 may be used, as appropriate, along withmultiple memories 862 of multiple types (e.g., a combination of a DSPand a microprocessor, a plurality of microprocessors, one or moremicroprocessors in conjunction with a DSP core).

Also, multiple computing devices may be connected, with each deviceproviding portions of the necessary operations (e.g., a server bank, agroup of blade servers, or a multi-processor system). Alternatively,some steps or methods may be performed by circuitry that is specific toa given function.

According to various embodiments, the computer system 800 may operate ina networked environment using logical connections to local and/or remotecomputing devices 820, 830, 840, 850 through a network 810. A computingdevice 830 may connect to a network 810 through a network interface unit896 connected to a bus 868. Computing devices may communicatecommunication media through wired networks, direct-wired connections orwirelessly, such as acoustic, RF, or infrared, through an antenna 897 incommunication with the network antenna 812 and the network interfaceunit 896, which may include digital signal processing circuitry whennecessary. The network interface unit 896 may provide for communicationsunder various modes or protocols.

In one or more exemplary aspects, the instructions may be implemented inhardware, software, firmware, or any combinations thereof. A computerreadable medium may provide volatile or non-volatile storage for one ormore sets of instructions, such as operating systems, data structures,program modules, applications, or other data embodying any one or moreof the methodologies or functions described herein. The computerreadable medium may include the memory 862, the processor 860, and/orthe storage media 890 and may be a single medium or multiple media(e.g., a centralized or distributed computer system) that store the oneor more sets of instructions 900. Non-transitory computer readable mediaincludes all computer readable media, with the sole exception being atransitory, propagating signal per se. The instructions 900 may furtherbe transmitted or received over the network 810 via the networkinterface unit 896 as communication media, which may include a modulateddata signal such as a carrier wave or other transport mechanism andincludes any delivery media. The term “modulated data signal” means asignal that has one or more of its characteristics changed or set in amanner as to encode information in the signal.

Storage devices 890 and memory 862 include, but are not limited to,volatile and non-volatile media such as cache, RAM, ROM, EPROM, EEPROM,FLASH memory, or other solid state memory technology; discs (e.g.,digital versatile discs (DVD), HD-DVD, BLU-RAY, compact disc (CD), orCD-ROM) or other optical storage; magnetic cassettes, magnetic tape,magnetic disk storage, floppy disks, or other magnetic storage devices;or any other medium that can be used to store the computer readableinstructions and which can be accessed by the computer system 800.

It is also contemplated that the computer system 800 may not include allof the components shown in FIG. 10 , may include other components thatare not explicitly shown in FIG. 10 , or may utilize an architecturecompletely different than that shown in FIG. 10 . The variousillustrative logical blocks, modules, elements, circuits, and algorithmsdescribed in connection with the embodiments disclosed herein may beimplemented as electronic hardware, computer software, or combinationsof both. To clearly illustrate this interchangeability of hardware andsoftware, various illustrative components, blocks, modules, circuits,and steps have been described above generally in terms of theirfunctionality. Whether such functionality is implemented as hardware orsoftware depends upon the particular application and design constraintsimposed on the overall system. Skilled artisans may implement thedescribed functionality in varying ways for each particular application(e.g., arranged in a different order or partitioned in a different way),but such implementation decisions should not be interpreted as causing adeparture from the scope of the present invention.

The above-mentioned examples are provided to serve the purpose ofclarifying the aspects of the invention, and it will be apparent to oneskilled in the art that they do not serve to limit the scope of theinvention. By way of example, the EAV device can be a traditional EAVdevice or a smart EAV device. By nature, this invention is highlyadjustable, customizable and adaptable. The above-mentioned examples arejust some of the many configurations that the mentioned components cantake on. All modifications and improvements have been deleted herein forthe sake of conciseness and readability but are properly within thescope of the present invention.

What is claimed is:
 1. A system for measuring galvanic skin response,comprising: an electrical conductivity meter electrically connected to apositive electrode and a negative electrode; and a server platform innetwork communication with the electrical conductivity meter; whereinthe electrical conductivity meter includes at least one processor and atleast one memory; wherein the negative electrode is configured to be incontact with a first portion of a subject and wherein the positiveelectrode is configured to be in contact with a second portion of thesubject, thereby creating a circuit including the positive electrode,the negative electrode, and the subject; wherein the electricalconductivity meter is configured to measure a galvanic skin response ofthe subject; wherein the positive electrode includes a pressure sensorconfigured to indicate an amount of pressure applied by a tip of thepositive electrode on a point of the subject; wherein the serverplatform includes software including a reasoning engine; and wherein thereasoning engine is configured to detect variations in the pressureapplied by the positive electrode.
 2. The system of claim 1, wherein thecircuit further includes a substance in contact with a test plate of theelectrical conductivity meter, and wherein the substance has been or iscurrently exposed to a stimulus, wherein the substance includes a food,a food component, a beverage, a supplement, a medication, a drug, anherb, a spice, a vitamin, a mineral, a gemstone, a metal, an electronicdevice, a bodily fluid, a tissue, and/or a hair sample.
 3. The system ofclaim 2, further comprising a device including a photon source and/or aTesla coil, wherein the device including the photon source and/or theTesla coil is configured to expose the substance to the stimulus, andwherein the stimulus includes electromagnetic waves.
 4. The system ofclaim 2, wherein the stimulus includes a biological output, or aresonance frequency of an animal or an organ of an animal.
 5. The systemof claim 2, wherein the stimulus includes mechanical waves.
 6. Thesystem of claim 2, wherein the electrical conductivity meter isconfigured to determine a galvanic skin measurement of the subject whenthe substance exposed to the stimulus is in contact with the test plateand thereby included in the circuit and a galvanic skin measurement ofthe subject when the substance exposed to the stimulus is not in contactwith the test plate and thereby not included in the circuit and whereinthe server platform is configured to compare the galvanic skinmeasurement of the subject when the substance exposed to the stimulus isin contact with the test plate and thereby included in the circuit, andthe galvanic skin measurement of the subject when the substance exposedto the stimulus is not in contact with the test plate and thereby notincluded in the circuit.
 7. The system of claim 6, wherein the serverplatform is configured to calculate a compatibility score for thesubstance exposed to the stimulus and the subject based on the galvanicskin measurement of the subject when the substance exposed to thestimulus is in contact with the test plate and thereby included in thecircuit, and the galvanic skin measurement of the subject when thesubstance exposed to the stimulus is not in contact with the test plateand thereby not included in the circuit, wherein the compatibility scoreindicates a degree of effectiveness, a degree of sensitivity, a degreeof tolerance, and/or a tendency to toxicity of the substance exposed tothe stimulus for the subject.
 8. The system of claim 1, furthercomprising a device configured to emit electromagnetic waves and/ormechanical waves, wherein the electrical conductivity meter isconfigured to determine a galvanic skin measurement of the subject whenthe subject is not exposed to the electromagnetic waves and/or themechanical waves, and is further configured to determine a galvanic skinmeasurement of the subject when the device exposes the subject to theelectromagnetic waves and/or the mechanical waves, and wherein theserver platform is configured to compare the galvanic skin measurementof the subject when the subject is not exposed to the electromagneticwaves and/or the mechanical waves, and the galvanic skin measurement ofthe subject when the subject is exposed to the electromagnetic wavesand/or the mechanical waves.
 9. The system of claim 8, wherein theserver platform is configured to calculate a compatibility score for theelectromagnetic waves and/or the mechanical waves and the subject basedon the galvanic skin measurement of the subject when the subject is notexposed to the electromagnetic waves and/or the mechanical waves, andthe galvanic skin measurement of the subject when the subject is exposedto the electromagnetic waves and/or the mechanical waves, wherein thecompatibility score indicates a degree of effectiveness, a degree ofsensitivity, a degree of tolerance, and/or a tendency to toxicity of theelectromagnetic waves and/or the mechanical waves for the subject. 10.The system of claim 8, wherein the electromagnetic waves and/or themechanical waves include sound and/or light.
 11. The system of claim 10,wherein the sound and/or light is constructed based on a biologicaloutput or a resonance frequency of an animal or an organ of an animal.12. The system of claim 8, wherein the mechanical waves include music,and wherein the music is selected based on a beats per minute (BPM)measurement of a biological output of an animal or an organ of an animalor a BPM measurement of a resonance frequency of the animal or the organof the animal.
 13. A system for measuring galvanic skin response,comprising: an electrical conductivity meter electrically connected to apositive electrode and a negative electrode; and a server platform innetwork communication with the electrical conductivity meter; whereinthe electrical conductivity meter includes at least one processor, atleast one memory, a display screen, and a test plate configured toreceive a substance exposed to electromagnetic waves and/or mechanicalwaves; wherein the negative electrode is configured to be in contactwith a first portion of a subject and wherein the positive electrode isconfigured to be in contact with a second portion of the subject,thereby creating a circuit including the positive electrode, thenegative electrode, and the subject; wherein the electrical conductivitymeter is configured to measure a galvanic skin response of the subject;wherein the circuit further includes the substance exposed to theelectromagnetic waves and/or the mechanical waves in contact with thetest plate; wherein the server platform is configured to calculate acompatibility score for the substance exposed to the electromagneticwaves and/or the mechanical waves and the subject based on a galvanicskin measurement of the subject when the substance exposed to theelectromagnetic waves and/or the mechanical waves is in contact with thetest plate and thereby included in the circuit, and a galvanic skinmeasurement of the subject when the substance exposed to theelectromagnetic waves and/or the mechanical waves is not in contact withthe test plate and thereby not included in the circuit, wherein thecompatibility score indicates a degree of effectiveness, a degree ofsensitivity, a degree of tolerance, and/or a tendency to toxicity of thesubstance exposed to the electromagnetic waves and/or the mechanicalwaves for the subject; and wherein the substance includes a food, a foodcomponent, a beverage, a supplement, a medication, a drug, an herb, aspice, a vitamin, a mineral, a gemstone, a metal, an electronic device,a bodily fluid, a tissue, and/or a hair sample.
 14. The system of claim13, wherein the electromagnetic waves and/or the mechanical wavesinclude sound and/or light.
 15. The system of claim 13, wherein thesubstance includes food, a food component, a coloring, an additive, apreservative, a thickener, a stabilizer, an emulsifier, an enhancer, abeverage, a supplement, a medication, a drug, an herb, a spice, avitamin, a mineral, a gemstone, a metal, an electronic device, a bodilyfluid, a tissue, and/or a hair sample.
 16. The system of claim 13,further comprising a device including a photon source and/or a Teslacoil, wherein the device including the photon source and/or the Teslacoil is configured to expose the substance to the electromagnetic waves.17. The system of claim 13, wherein the mechanical waves include music,and wherein the music is selected based on a beats per minute (BPM)measurement of a biological output of an animal or an organ of an animalor a BPM measurement of a resonance frequency of the animal or the organof the animal.
 18. A system for measuring galvanic skin response,comprising: an electrical conductivity meter electrically connected to apositive electrode and a negative electrode; a server platform innetwork communication with the electrical conductivity meter; and adevice including a photon source and/or a Tesla coil configured to emitelectromagnetic waves; wherein the electrical conductivity meterincludes at least one processor, at least one memory, a display screen,and a test plate configured to receive a substance exposed to theelectromagnetic waves and/or mechanical waves; wherein the negativeelectrode is configured to be in contact with a first portion of asubject and wherein the positive electrode is configured to be incontact with a second portion of a subject, thereby creating a circuitincluding the positive electrode, the negative electrode, and thesubject; wherein the electrical conductivity meter is configured tomeasure a galvanic skin response of the subject; wherein the circuitfurther includes the substance exposed to the electromagnetic wavesand/or the mechanical waves in contact with the test plate; wherein theserver platform is configured to calculate a compatibility score for thesubstance exposed to the electromagnetic waves and/or the mechanicalwaves and the subject based on a galvanic skin measurement of thesubject when the substance exposed to the electromagnetic waves and/orthe mechanical waves is in contact with the test plate and a galvanicskin measurement of the subject when the substance exposed to theelectromagnetic waves and/or the mechanical waves is not in contact withthe test plate, wherein the compatibility score indicates a degree ofeffectiveness, a degree of sensitivity, a degree of tolerance, and/or atendency to toxicity of the substance exposed to the electromagneticwaves and/or the mechanical waves for the subject; wherein the deviceincluding the photon source and/or the Tesla coil is configured toexpose the substance to the electromagnetic waves; and wherein thesubstance includes a food, a food component, a coloring, an additive, apreservative, a thickener, a stabilizer, an emulsifier, an enhancer, abeverage, a supplement, a medication, a drug, an herb, a spice, avitamin, a mineral, a gemstone, a metal, an electronic device, a bodilyfluid, a tissue, and/or a hair sample.
 19. The system of claim 18:further comprising a hydration sensor configured to measure a level ofhydration of the subject; wherein the test plate is formed of metal;wherein the test plate includes at least one cylindrical hole configuredto hold an ampule or a vial of the substance exposed to theelectromagnetic waves and/or the mechanical waves; wherein theelectrical conductivity meter applies a measurement current of less than12 μA; wherein the positive electrode has a brass tip and/or a silvertip; wherein the server platform includes software including a reasoningengine, wherein the reasoning engine includes artificial intelligence(AI) algorithms configured to detect variations in pressure applied bythe positive electrode during a single session, across multiple sessionswith a single subject, or across multiple sessions with multiplesubjects.